MEDICAL ACTION INDUSTRIES 77433Recalls & reported problems
Medical Action Industries Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10809160189887), received between Sep 16, 2021 and Sep 15, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Contamination” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Contamination1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2023
CHLORAPREP IN CVC REDRESS KIT WAS DRY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17755291 ↗MalfunctionSep 16, 2021Contamination
OPENED UP A STERILE CVC REDRESS KIT AND A HAIR WAS FOUND LAYING ON TOP OF THE MASK. OBTAINED A NEW KIT TO ACCESS PORT ON PREOP PATIENT. PRODUCT AND PACKAGING SAVED.
Patient problems: Insufficient Information
MAUDE report 12480380 ↗
Other Central venous catheter dressing change kit devices
- Medical Action Industries 59816BMedical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- Medical Action Industries 79544BMedical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- MEDICAL ACTION INDUSTRIES 79420Medical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- Medical Action Industries 74564Medical Action Industries Inc. · Central venous catheter dressing change kit3 reports
- Medical Action Industries 58193Medical Action Industries Inc. · Central venous catheter dressing change kit1 report
- medical action industries 77993DMedical Action Industries Inc. · Central venous catheter dressing change kit1 report
- Medical Action Industries 75911DMedical Action Industries Inc. · Central venous catheter dressing change kit1 report
- McKesson 25-2835Mckesson Medical-Surgical Inc. · Central Venous Catheter Dressing Change Kit1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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